|Publication number||US20060009858 A1|
|Application number||US 11/057,861|
|Publication date||Jan 12, 2006|
|Filing date||Feb 14, 2005|
|Priority date||Jul 9, 2004|
|Also published as||DE602005027570D1, EP1768618A1, EP1768618B1, US7837643, WO2006016894A1|
|Publication number||057861, 11057861, US 2006/0009858 A1, US 2006/009858 A1, US 20060009858 A1, US 20060009858A1, US 2006009858 A1, US 2006009858A1, US-A1-20060009858, US-A1-2006009858, US2006/0009858A1, US2006/009858A1, US20060009858 A1, US20060009858A1, US2006009858 A1, US2006009858A1|
|Inventors||Andy Levine, David Melanson, Ronald Lamport|
|Original Assignee||Gi Dynamics, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (98), Referenced by (106), Classifications (16), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application claims the benefit of U.S. Provisional Application No. 60/586,521, entitled “Methods and Articles for Placement and Removal of Gastrointestinal Sleeves” and filed on Jul. 9, 2004, and U.S. Provisional Application No. 60/610,614, entitled “Methods and Articles for Placement and Removal of Gastrointestinal Sleeves” and filed on Sep. 15, 2004. The teachings of these provisional applications are incorporated herein by reference.
Obesity is an overwhelming health problem. According to the Center for Disease Control (CDC), over sixty percent of the United States population is overweight, and almost twenty percent are obese. This translates into about 40 million adults in the United States with a Body Mass Index (BMI) of 30 or above. The BMI is defined as a person's weight (in kilograms) divided by height (in meters), squared. To be considered clinically, morbidly obese, one must meet one of three criteria: a Body Mass Index of more than 35, one hundred pounds overweight, or 100% above ideal body weight. There is also a category for the super-obese for those weighing over 350 lbs.
Carrying this excess weight places enormous strain upon a person's body; organs are affected, as are the nervous and circulatory systems. In 2000, the National Institute of Diabetes, Digestive and Kidney Diseases (NIDDK) estimated that there were 280,000 deaths directly related to obesity. The NIDDK further estimated that the direct cost of healthcare in the US associated with obesity is $51 billion. In addition, Americans spend $33 billion per year on weight loss products. In spite of this economic cost and consumer commitment, the prevalence of obesity continues to rise at alarming rates. From 1991 to 2000, obesity rates in the US grew by 61% and worldwide obesity rates also increased dramatically.
One of the principle costs to the healthcare system stems from the co-morbidities associated with obesity. Incidence of Type-2 diabetes has climbed to 7.3% of the population. Of those persons with Type-2 diabetes, almost half are clinically obese, and two thirds are approaching obese. Other co-morbidities include hypertension, coronary artery disease, hypercholesteremia, sleep apnea and pulmonary hypertension.
Although the physiology and psychology of obesity are complex, the medical consensus is that the cause is quite simple: over consumption of calories combined with a reduction in energy expenditures seen in modern society. While the treatment seems quite intuitive, the institution of a cure is a complex issue that has so far vexed the best efforts of medical science. Dieting is not an adequate long-term solution for most people. Once an individual has slipped past the BMI of 30, significant changes in lifestyle are the only solution.
There have been many attempts in the past to surgically modify patients' anatomies to attack the consumption problem by reducing the desire to eat. Stomach saplings, or gastroplasties, to reduce the volumetric size of the stomach, therein achieving faster satiety, were performed in the 1980's and early 1990's. Although able to achieve early weight loss, sustained reduction was not obtained. The reasons are not all known, but are believed related to several factors. One of which is that the stomach stretches over time increasing volume while psychological drivers motivate patients to find creative approaches to literally eat around the smaller pouch.
There are currently two surgical procedures that successfully produce long-term weight loss; the Roux-en-Y gastric bypass and the biliopancreatic diversion with duodenal switch (BPD). Both procedures reduce the size of the stomach plus shorten the effective-length of intestine available for nutrient absorption. Reduction of the stomach size reduces stomach capacity and the ability of the patient to take in food. Bypassing the duodenum makes it more difficult to digest fats, high sugar and carbohydrate rich foods. One objective of the surgery is to provide feedback to the patient by producing a dumping syndrome if they do eat these food products. Dumping occurs when carbohydrates directly enter the jejunum without being first conditioned in the duodenum. The result is that a large quantity of fluid is discharged into the food from the intestinal lining. The total effect makes the patient feel light-headed and results in severe diarrhea. For reasons that have not been determined the procedure also has an immediate therapeutic effect on diabetes.
Although the physiology seems simple, the exact mechanism of action in these procedures is not understood. Current theory is that negative feedback is provided from both regurgitation into the esophagus and dumping when large volumes of the wrong foods are eaten. Eventually, patients learn that to avoid both these issues they must be compliant with the dietary restrictions imposed by their modified anatomy. In the BPD procedure, large lengths of jejunum are bypassed resulting in malabsorption and therefore, reduced caloric uptake. In fact, the stomach is not reduced in size as much in the BPD procedure so that the patient is able to consume sufficient quantities of food to compensate for the reduced absorption. This procedure is reserved for the most morbidly obese as there are several serious side effects of prolonged malabsorption.
Unfortunately, these procedures carry a heavy toll. The morbidity rate for surgical procedures is alarmingly high with 11% requiring surgical intervention for correction. Early small bowel obstruction occurs at a rate of between 2-6% in these surgeries and mortality rates are reported to be approximately 0.5-1.5%. While surgery seems to be an effective answer, the current invasive procedures are not acceptable with these complication rates. Laparoscopic techniques applied to these surgeries provide fewer surgical complications but continue to expose these very ill patients to high operative risk in addition to requiring an enormous level of skill by the surgeon. Devices to reduce absorption in the small intestines have been proposed (See U.S. Pat. No. 5,820,584 (Crabb), U.S. Pat. No. 5,306,300 (Berry) and U.S. Pat. No. 4,315,509 (Smit)). However, these devices have not been successfully implemented.
Recently, various gastrointestinal implants have been developed as potential solutions to these above problems. However, a need exists for methods and devices to place or position these implants within mammalian gastrointestinal tracts.
This invention is directed towards methods, devices, and systems for implanting or placing a gastrointestinal implant device (e.g., a gastrointestinal sleeve) into the gastrointestinal tract of a mammal (e.g., a human). The methods utilize, and the devices include, a container assembly and a gastrointestinal implant device having a proximal end that includes an anchor and a distal end that includes a sleeve.
This invention includes methods of placing a gastrointestinal implant device in a mammal. The gastrointestinal implant device includes an anchor and a flexible, floppy, thin, conformable, and/or collapsible sleeve sleeve. In some embodiments, the method comprises the steps of placing a gastrointestinal implant device in a container assembly, directing the container assembly into a mammalian gastrointestinal tract, removing the device from the container assembly, and securing the anchor to a location in the gastrointestinal tract. In some embodiments of the invention, the step of removing the device from the container assembly includes directing a portion of the sleeve to a location in the gastrointestinal tract that is distal relative to the assembly while the anchor is releasably secured in the container assembly.
In some embodiments, at least a portion of the sleeve is removed from the container assembly before the anchor is removed from the container. Optionally, the anchor is releasably secured in the container assembly while at least a portion of the sleeve is directed to a location in the gastrointestinal tract that is distal from the container assembly. The sleeve can be directed into the location by, for example, advancing a catheter having an atraumatic tip. In further embodiments, a distal portion of the catheter is less rigid than a proximal portion of the catheter.
In some embodiments of the invention, the container is directed to the duodenum of the gastrointestinal tract. In further embodiments, at least a portion of the sleeve is directed into the jejunum of the gastrointestinal tract. Optionally, the anchor is self-expanding and/or is secured in the duodenum of the gastrointestinal tract.
In some embodiments of the invention, the method further includes a step of directing a fluid (e.g., a gas and/or liquid) into the gastrointestinal tract. The fluid can be directed into the tract before and/or after the container assembly is directed into the duodenum. The fluid can be used, for example, to expand at least a portion of the gastrointestinal tract and/or to deploy or expand portions of the gastrointestinal implant device. Examples of suitable fluids include gasses (e.g., air, carbon dioxide, and/or nitrogen) and liquids (e.g., saline and mixtures of liquid saline and a contrast medium). In some embodiments, at least 60 milliliters of fluid are directed into the gastrointestinal tract.
In some embodiments of the invention, the container assembly includes a first chamber and the step of placing the device in the assembly includes storing the anchor in the first chamber. Optionally, the step of removing the device from the assembly includes directing at least a portion of the sleeve to a location in the gastrointestinal tract that is distal relative to the first chamber while the anchor is releasably secured in the first chamber. In further embodiments of the invention, the container assembly further includes a second chamber and the step of placing the device in the assembly includes storing at least a portion of the sleeve in the second chamber. Optionally, the step of removing the device from the assembly includes directing the second chamber to a location in the gastrointestinal tract that is distal relative to the first chamber while the anchor is releasably secured in the first chamber and the sleeve is releasably secured in the second chamber.
This invention also includes delivery systems for placing a gastrointestinal implant device in a mammalian gastrointestinal tract. In some embodiments of the invention, the delivery systems comprise a container assembly and a gastrointestinal implant device. The implant device includes a proximal end and a distal end, and the proximal end includes an anchor and the distal end includes a sleeve. The proximal end and the distal end are stored within the container assembly.
In further embodiments, the systems include an anchor locking mechanism located within the assembly. The anchor locking mechanism can include an anchor locking wire that extends through a portion of the device. The system can further include a means for displacing an anchor from the container assembly (e.g., an anchor plunger). Optionally, the anchor is self-expanding. The exterior portion of the container assembly can include a visible marker for positioning the assembly within the gastrointestinal tract of a mammal.
In additional embodiments, the systems further include a catheter releasably secured to the distal end of the device. For example, the catheter can be releasably secured to the distal end of the sleeve. The catheter can include an atraumatic tip (e.g., a releasable ball) and/or a distal portion of the catheter can be less rigid than a proximal portion of the catheter.
In some embodiments, wherein the assembly includes a first chamber and a second chamber, the first chamber storing at least a portion of the proximal end and the second chamber storing at least a portion of the distal end. In further embodiments, at least a portion of the second chamber is stored in the first chamber.
The foregoing and other objects, features and advantages of the invention will be apparent from the following more particular description of preferred embodiments of the invention, as illustrated in the accompanying drawings in which like reference characters refer to the same parts throughout the different views. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the invention.
A description of preferred embodiments of the invention follows. While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.
This invention features devices and methods for implanting or placing gastrointestinal implant devices (e.g., intestinal sleeves) into mammals (e.g., a human). Several gastrointestinal implant devices (e.g., intestinal sleeves) have been developed and are suitable for implementation or placement within a gastrointestinal tract using the methods and devices of this invention. Some examples of such devices are described in U.S. patent application Ser. No. 10/339,786, filed Jan. 9, 2003, and entitled “Bariatric Sleeve;” U.S. patent application Ser. No. 10/726,011, filed Dec. 2, 2003, and entitled “Anti-Obesity Devices;” U.S. patent application Ser. No. 10/810,317, filed Mar. 26, 2004, and entitled “Enzyme Sleeve;” U.S. patent application Ser. No. 10/811,293, filed Mar. 26, 2004, and entitled “Anti-Obesity Devices;” U.S. patent application Ser. No. 10/858,852, filed Jun. 1, 2004, and entitled “Methods and Apparatus for Anchoring Within the Gastrointestinal Tract;” U.S. Provisional Application No. 60/544,527, filed Feb. 13, 2004, and entitled “Methods and Apparatus for Using a Sleeve Within the Gastrointestinal Tract;” U.S. patent application Ser. No. 10/858,851, filed Jun. 1, 2004, and entitled “Intestinal Sleeve;” U.S. Patent Application No. 60/611,038, filed Sep. 17, 2004, and entitled “Multi-Wave Anchor;” U.S. Provisional Application No. 60/645,296, filed on Jan. 19, 2005, and entitled “Gastrointestinal Sleeve;” and U.S. Provisional Application No. 60/645,287, filed Jan. 19, 2005, entitled “Anchoring Devices.” The teachings of each of these applications are incorporated herein by reference.
The pylorus 108 is a distal aperture of the stomach 102 surrounded by a strong band of circular muscle. The small intestine, about 15-20 feet in length, is a convoluted tube, extending from the pylorus 108 to the ileo-caecal valve where it terminates in the large intestine. The small intestine has three sections, the duodenum 104, jejunum 106 and the ileum (not shown in
The duodenum 104 has four sections which typically form a U shape: superior, descending, transverse, and ascending. The superior section is about two inches long and ends at the neck of the gall bladder. The superior section also defines a feature referred to as the duodenal bulb 119 that begins just distal to the pylorus 108 and extends for about 1 to 1.5 inches in an adult human. The duodenal bulb 119 defines a lumen therein that is slightly larger than the distal duodenum 104. Advantageously, the duodenal bulb 119 exhibits less motion than the pylorus 108 and even distal portions of the duodenum 104. Notably, the motion is substantially limited to contractions without having a significant linear component (i.e., no movement along the central axis of the intestine). The tissue of the intestinal wall of the pylorus 108, and to some extent that of the duodenal bulb 119, tends to be thicker than that of other portions of the small intestine, but the tissue thins as one moves away from the pylorus 108.
The descending section of the duodenum 104 is about three to four inches long and includes a nipple shaped structure, the papilla of Vater 114, through which pancreatic juice from the pancreas and bile produced by the liver and stored by the gall bladder enter the duodenum from the pancreatic and bile ducts. The pancreatic juice contains enzymes essential to protein digestion and bile dissolves the products of fat digestion. The ascending section is about two inches long and forms the duodenal-jejunal flexure 116 where it joins the jejunum 106, the next section of the small intestine. The duodenal-jejunal flexure 116 is fixed to the ligament of Treitz 118 (musculus supensionus duodeni). The juices secreted in the duodenum break the partially digested food down into particles small enough to be absorbed by the body. The digestive system is described in Gray's Anatomy (“Anatomy of the Human Body,” by Henry Gray) and “Human Physiology,” Vander, 3rd ed, McGraw Hill, 1980, the contents of which are incorporated herein by reference in their entirety.
This invention includes methods and devices for placing or implanting a gastrointestinal implant device in a mammal. For example, this invention includes methods and devices for implanting a gastrointestinal sleeve. In some embodiments, the gastrointestinal sleeve includes an anchor portion and a floppy, flexible, thin, conformable, and/or collapsible sleeve portion.
Anchor 152 can be removably attached within the body using the methods described herein, including the use of barbs attached to, and/or formed on, the anchor itself. In some embodiments, the anchor is attached or secured within the gastrointestinal tract without the use of barbs. When implanted, anchor 152 allows sleeve 154 to be securely implanted within the duodenum, preferably providing a fluid seal at the proximal end.
In some embodiments, the device is anchored in the bulbous duodenum. For purposes of anchoring a gastrointestinal device, the bulbous duodenum offers several advantages over other areas in of gastrointestinal tract. First, the duodenal bulb is proportionally sized to capture an anchor. That is, it provides a cavity having a relatively large diameter bounded by anatomies having smaller diameters in both the proximal and distal directions. Thus, the duodenal bulb is naturally configured to retain a suitably shaped anchor. Additionally, the duodenal bulb is relatively less active than either the pylorus or the distal portions of the duodenum. Movement of the surrounding tissue can act to dislodge an anchor over time. The duodenal bulb, at least in part, acts as a holding area for chyme received from the stomach. Thus, the duodenal bulb provides a more stable anchoring platform as there is relatively less movement than at other portions of the gastrointestinal tract. Still further, the tissue of at least the proximal portion of the duodenal bulb is thicker than the tissue of the distal duodenum, thus, the duodenal bulb provides a better anchoring platform as it is adapted to retain fasteners (e.g., barbs).
Optionally, a proximal portion of the small intestine (e.g., the duodenum) is expanded in order to create a working space for the practitioner. One method of expanding a proximal portion of the small intestine is to direct a fluid into the duodenum via a working channel in the gastro-scope. Examples of suitable fluids include gases (e.g., air, nitrogen, and/or carbon dioxide) or liquids (e.g., water and/or saline). In some embodiments, the fluid is a liquid mixture of saline and a contrast medium. Examples of suitable contrast mediums include a fluorescent material, a radiopaque material, or a contrast medium commonly used for intravenous urography (e.g., preparations of diatrizoate sodium and diatrizoate meglumine). In still further embodiments, the liquid is a mixture of about 75% saline and about 25% Renografin™ (available from Bracco Diagnostics, Inc. Corporation, East Princeton, N.J.).
The exact amount of fluid needed to sufficiently expand the duodenum will depend on variables such as the size of the patient's gastrointestinal tract, the preferences of the practitioner, and/or the length of the gastrointestinal device to be delivered. In some embodiments, at least 60 milliliters of a fluid are used to expand the duodenum. In further embodiments, at least 200 milliliters of a fluid are used to expand the duodenum. 200 milliliters of a fluid would be useful for delivering, for example, a gastrointestinal sleeve that is about two feet in length. In further embodiments, at least 500 milliliters of a fluid are used to expand the duodenum. In still further embodiments, about 600 milliliters of a fluid are used to expand the duodenum which would be useful for delivering, for example, a gastrointestinal sleeve that is about 4 feet in length.
After the small intestine has been expanded to the desired extent, a length of guidewire 214 is directed through the working channel of gastro-scope 202, out of the distal end 208, and into the proximal portion of the duodenum, as illustrated in
Once the guidewire is in the desired location and the gastro-scope has been removed, a delivery catheter is directed into the duodenum, as illustrated in
Alternatively, in some embodiments of the invention, the container assembly is advanced into the stomach and the guidewire is removed. A gastro-scope is used to direct the container assembly partially or entirely through the pylorus and into the small intestine.
Once container 216 is at the desired location in the duodenum, guidewire 214 can be removed from the gastrointestinal tract, as illustrated in
The container holds or houses parts or all of a gastrointestinal implant device (e.g., a gastrointestinal sleeve). The gastrointestinal implant device includes a distal portion and a proximal portion. The distal portion includes a gastrointestinal sleeve and the proximal portion of the device includes an anchor for securing the device within the gastrointestinal tract (e.g., in the proximal duodenum). In some embodiments, the container holds or houses the proximal portion of the gastrointestinal device. In other embodiments, the container holds or houses both the distal and proximal portions. In still further embodiments, the container holds or houses the entire gastrointestinal device. Some or all of the sleeve portion can be folded and stored in the container with the anchor.
After container 216 is at the desired location in the proximal duodenum, a distal portion 222 of the sleeve is removed from the container and directed into a location in the gastrointestinal tract that is distal from the container, as illustrated in
Distal portion 222 of the sleeve is releasably secured to the leading or distal portion of the inner catheter so that as the inner catheter is advanced through the distal intestine, distal portion 222 is also advanced. In this manner, distal portion 222 is directed to locations in the gastrointestinal tract that are distal from container 216 and into the distal intestines (e.g., into the jejunum).
As the inner catheter is advanced through the inner catheter lumen and into the distal intestine, the proximal portion (not illustrated in
The distal end of the inner catheter includes or is attached to an atraumatic tip (e.g., atraumatic ball 220), which minimizes or eliminates tissue trauma as the inner catheter is advanced into the distal intestines. The exact location to which distal portion 222 is advanced into the distal intestines will vary with the needs of the patient and the demands of the given procedure. The inner catheter also includes a stiffening wire that provides sufficient linear or column strength to the inner catheter to facilitates navigation of the distal intestines. Optionally, fluoroscopy is used to track the progress of the advancement.
After the desired length of sleeve has been delivered, endoscope 224 is optionally directed into the stomach to visually inspect the proximal end of delivery capsule 216 to ensure that it is in the desired position and/or to monitor the subsequent anchor deployment process, as illustrated in
After the distal portion of the sleeve is advanced to a desired location in the distal intestines, the anchor is deployed from the container and secured to a desired position within the gastrointestinal tract, as illustrated in
Container 216 includes visual marker 230 (e.g., a black ring) that can be used to determine if the capsule is in a desired location before anchor 228 is fully removed from container 216 and secured at a desired location in the gastrointestinal tract. For example, delivery catheter 218 is pulled proximally until visual marker 230 is proximal to pylorus 206 and visible in the stomach to endoscope 224. In this manner, the practitioner can ensure that the anchor will deploy at the desired anchoring position when it is removed from container 216.
Once container 216 is in the desired location, outer catheter 218 is held in position and the inner catheter is advanced further distally to pull the sleeve and anchor 228 from container 216. Optionally, the anchor is pushed out of the container using a means for displacing an anchor from the container assembly (e.g., an anchor plunger).
As shown in
After anchor 228 is deployed and the device secured within the gastrointestinal tract, endoscope 224 is optionally removed and/or the stiffening wire is pulled proximally through a main stiffening wire lumen defined by inner catheter 229 and removed from the gastrointestinal tract. After the stiffening wire has been removed, the sleeve is optionally expanded or inflated by directing fluid through the main stiffening wire lumen defined by inner catheter 229, as illustrated in
Inner catheter 229 and outer catheter 218 are removed, as illustrated in
Optionally, the endoscope is positioned across the pylorus and a fluid (e.g., a gas or liquid, such as air, nitrogen, carbon dioxide, saline, or dilute Renografin™) is directed into the duodenum to confirm patency of the sleeve, as illustrated in
In some embodiments of the invention, the gastrointestinal implant devices are implanted via catheter-based placements methods (e.g., within endoluminal catheter).
Inner and outer catheters 310, 306 and container 304 are made from materials commonly used to form catheters. For example, inner catheter 310 can be made of a polyether block amide (e.g., Pebax® 7233, available from Arkema Group, Paris, France). In some embodiments, outer catheter 306 is made of high density polyethylene and/or container 304 is made of hard plastic (e.g., acetal or polycarbonate). Preferably, catheters 310, 306 are made from materials having frictional properties that facilitate the movement of catheter 310 relative to catheter 306 and facilitate the movement of inner catheter 310 and container 304 in the gastrointestinal tract.
Turning back to
Outer catheter 306 includes anchor locking wire port 336, anchor plunger port 340, and attachment port 342 at proximal end 346.
Turning back to
System 300 includes inner catheter pusher 308. Inner catheter pusher 308 is assembled or attached to outer catheter 306.
In operation, depressing locking handle 368 causes locking pads 362 to securely grip a portion of inner catheter 310 relative to handle 368 and slide tube 360. Applying force in direction 366 while handle 368 is depressed moves handle 368, tube 360, and inner catheter 310 relative to handle 358, thereby directing a length of inner catheter 310 into the inner catheter lumen defined by the outer catheter. After pressure is released from handle 368, handle return spring 364 causes locking pads 362 to disengage from inner catheter 310. Once disengaged from inner catheter 310, handle 368 is moved along direction 367, and the process can then be repeated. In this manner, inner catheter 310 can be advanced distally through inner catheter lumen 350 defined by outer catheter 306. Slide tube 360 provides rigid support to inner catheter 310 to prevent inner catheter 310 from kinking during advancement.
System 400 includes an atraumatic tip comprising atraumatic ball 402, a container assembly that includes capsule or container 404, outer catheter 406, inner catheter pusher 408, inner catheter 410, and guidewire 412.
In some embodiments of this invention, system 400 is used to place or install a gastrointestinal implant device (e.g., a gastrointestinal sleeve) into the digestive tract of a mammal. Briefly, a gastrointestinal sleeve is releasably secured to the distal end of inner catheter 410 with a locking wire and then the sleeve and an anchor portion is placed or stored within container 404 of a container assembly. Guidewire 412 is directed into a desired location within a gastrointestinal tract of a mammal (e.g., in a proximal portion of the small intestine). After guidewire 412 is in the desired location, container 404 is directed along the guidewire into a desired location within the mammal's gastrointestinal tract (e.g., the duodenum). The distal end of inner catheter 410, along with the secured portion of the gastrointestinal sleeve, is advanced within the gastrointestinal tract to a location that is distal from container 404, thereby extending or unfurling at least a portion of the gastrointestinal sleeve. During some or all of the unfurling portion of the procedure, the anchor and the proximal portion of the sleeve is releasably secured within the container assembly with a locking wire. Once the sleeve has been extended to the desired extent (e.g., into the jejunum), the anchor portion is unlocked from the container assembly and removed from the container. The anchor can be removed from container 404 by, for example, again advancing inner catheter 410 and the releasably secured distal end of the sleeve, thereby pulling the unlocked anchor from container 404. Optionally, the anchor is removed from container 404 with the use of a means for displacing an anchor from the container assembly that includes anchor plunger 411. The anchor is secured at desired location within the gastrointestinal tract of the mammal (e.g., in the duodenum). Any portion of the gastrointestinal implant device that is still secured to system 400 is detached, and the system is removed from the mammal.
After the distal end of guidewire 412 is directed to a desired location within the gastrointestinal tract of a mammal, the proximal end of guidewire 412 is directed through a guidewire lumen defined by container 404. Once assembled to guidewire 412, outer catheter 406 is advanced to direct container 404 along guidewire 412 and to a desired location within the gastrointestinal tract of the mammal. After container 404 has been advanced to the desired location, guidewire 412 is removed from the gastrointestinal tract of the mammal.
Inner catheter pusher 408 is used to direct a distal end of inner catheter 410 into a desired location in the gastrointestinal tract that is distal to container 404. Locking handle 414 is depressed, thereby causing the pads (not illustrated in
In some embodiments, the inner catheter includes an atraumatic tip (e.g., a releasable or deflatable atraumatic ball tip) which facilitates the advancement of the inner catheter through the gastrointestinal tract (e.g., through the proximal intestines). The atraumatic tip allows the inner catheter to be advanced through a gastrointestinal tract, while reducing or eliminating damage or irritation to tissue. The atraumatic tip guides the inner catheter through the distal intestines. The atraumatic ball is in the range of between about 5 millimeters and about 20 millimeters. Preferably, the ball tip is in the range of between about 6.4 millimeters and about 19.2 millimeters in diameter. Most preferably, the atraumatic ball is about 12.7 millimeters in diameter.
Inner catheter 410 defines tension wire lumen 432. The tension wire provides structural support to inner catheter 410 to prevent unwanted deformations of catheter 410 during insertion or maneuverings within a gastrointestinal tract. For example, the tension wire can be included to prevent inner catheter 410 from elongating or stretching. Such elongating or stretching can cause locking wire 422 to emerge from port 428 prematurely, thereby releasing distal ball 402 and distal portion 420 from distal end 418 at undesirable portions of a placement procedure.
Container 404 is attached or assembled to outer catheter 406 (a portion of which is omitted from
The proximal end of the gastrointestinal device includes one or more drawstrings which are attached to the proximal end of the device via perforations in the sleeve material. In some embodiments, one or more of these drawstrings are used to releasably secure or lock anchor 452 within container 404. For example, anchor retaining wire 421 extends out of the proximal end of container 404 via anchor retaining wire port 423 defined by anchor pusher plate 411 and container 404. Anchor locking wire 440 extends through anchor locking wire lumen 427 which is defined by outer catheter 406. Wire 440 emerges from lumen 427 via anchor locking wire port 438, extends through drawstring 421, and extends back into lumen 427 via anchor locking wire port 439.
After sleeve 416 has been deployed to a desired extent and container 404 is in the desired location, anchor 452 and the proximal portion of sleeve 416 can be released from container 404.
Once anchor 452 has been released from anchor locking wire 440, anchor 452 and proximal portion of sleeve 416 are expelled from container 404. To expel anchor 452 and the proximal portion of sleeve 416, a practitioner pushes anchor pusher wire 444 distally, thereby directing plate 411 along a direction parallel to direction 458 and forcing anchor 452 from the distal end of container 404. Optionally, or in addition, inner catheter 410 is advanced further, thereby causing distal portion 420 of sleeve 416 and the attached anchor 452 to advance distally relative to container 404 until anchor 452 emerges from container 404. In some embodiments, one or more of the chambers of the container assembly is lined with a layer of metal or metal alloy, thereby preventing portions of the anchor from adhering to the inner container walls and facilitating removal of the anchor from the container assembly.
Moving stop 454 is attached to, or formed by a portion of, wire 444 and has an outer diameter that is greater than the outer diameter of the portions of wire 444 that are distal from stop 454. Moving stop 454 moves or translates with wire 444 relative to outer catheter 406 along a direction that is parallel to direction 458.
Static stop 456 is attached to, or formed by a portion of, outer catheter 406. Stop 456 remains stationary with respect to catheter 406 as wire 444 is translated distally. Static stop 456 defines an inner diameter that is less than the diameter of moving stop 454 but greater than the diameter of the portion of wire 444 that is distal to moving stop 454. Hence, when wire 444 is sufficiently translated distally along a direction parallel to direction 458, moving stop 454 contacts static stop 456, thereby preventing further distal translation of wire 444 along a direction parallel to direction 458. In this manner, the mechanism allows a practitioner of the invention to sufficiently translate plate 411 distally so as to expel a gastrointestinal implant device from a container while simultaneously preventing plate 411 from emerging form the distal end of the container.
After anchor 452 is free of container 405, anchor 452 expands and is secured to a desired location within the gastrointestinal tract.
After anchor 452 has been deployed, distal portion 420 of sleeve 416 and ball 402 can be released from distal end 418 of inner catheter 410.
Optionally, a fluid (e.g., a gas or liquid) is directed into the gastrointestinal sleeve after the anchor has been deployed. At such a point in a placement process, stiffening wire 436 is no longer needed and can be removed from system 400 by pulling wire 436 proximally at stiffening wire port 446, and removing it entirely from stiffening wire lumen 434. Optionally, a fluid can then be directed through lumen 434 and into sleeve 416, thereby expanding at least a portion of sleeve 416.
In some embodiments of this invention, two capsules or containers are used to deliver or place a gastrointestinal device into a mammal.
Before insertion into a mammalian body, the distal end of sleeve 608 is secured or fastened inside of second container 604, while the anchor is secured or fastened within first container 602. A portion of the sleeve is also bundled into second container 604. Second container 604, including sleeve 608 is then placed inside of first container 602. First container 602 is attached to outer catheter 610 and inserted into the proximal duodenum. Second container 604 is attached to the distal end of the inner catheter. Second container 604 is advanced into the distal intestine along with the distal end of inner catheter and atraumatic ball 606. As second container 604 is advanced, sleeve 608 is released from the proximal end of second container 604. Once the distal end of the inner catheter is advanced to the desired location in the distal intestines, the distal end of sleeve 608 is unlocked from the first container. The anchor is then released from first container 602 and the device is secured within the gastrointestinal tract. The second container and atraumatic ball are passed through the digestive tract via natural peristalsis. Optionally, the second container and the atraumatic ball are formed from a single piece of material.
The ends of a wire, or thread 4600 are attached to ball 4218 and thread 4600 is looped through sleeve retention wire 4208 to hold ball 4218 at the distal end of inner shaft 4200 of the catheter. Ball 4218 is released by pulling back on sleeve retention wire 4208 with fitting 4200 (
Ball 4218 includes two holes 4800, 4802 extending from recess 4706 to exterior surface of ball 4218. The distal end of sleeve retention wire 4208 passes through hole 166 and is looped back into hole 167. As sleeve retention wire 4208 is pulled proximally, wire 4218 is pulled back through hole 4802 and then through hold 4800 and ball 4218 is released from the distal end of the catheter.
The distal end of a delivery catheter (e.g., an inner catheter) can includes an atraumatic tip comprising a low profile balloon instead of a releasable ball.
While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.
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|U.S. Classification||623/23.65, 606/108|
|International Classification||A61F5/00, A61M25/01, A61F2/04|
|Cooperative Classification||A61F5/0076, A61F2002/9517, A61F2002/044, A61F5/0089, A61F2002/045, A61F2/04, A61F2/95|
|European Classification||A61F2/95, A61F2/04, A61F5/00B8, A61F5/00B6N|
|Apr 12, 2005||AS||Assignment|
Owner name: G.I. DYNAMICS, INC., MASSACHUSETTS
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LEVINE, ANDY H.;MELANSON, DAVID A.;LAMPORT, RONALD B.;REEL/FRAME:016057/0351;SIGNING DATES FROM 20050318 TO 20050319
|Aug 10, 2005||AS||Assignment|
Owner name: GI DYNAMICS, INC., MASSACHUSETTS
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LEVINE, ANDY H.;MELANSON, DAVID A.;LAMPORT, RONALD B.;REEL/FRAME:016631/0925;SIGNING DATES FROM 20050318 TO 20050319
|Apr 22, 2014||FPAY||Fee payment|
Year of fee payment: 4